Quality Control & Quality Affairs (QC/QA) Associate II

Quality Control & Quality Affairs (QC/QA) Associate II Quicksilver Scientific, Inc - 3.9 Louisville, CO Job Details Full-time $30 - $33 an hour 2 hours ago Benefits Health savings account Disability insurance Health insurance Dental insurance Flexible spending account Paid time off 401(k) 4% Match Vision insurance 401(k) matching Gym membership Qualifications GMP Productivity software Full Job Description Join Our Team as a Quality ControlQuality Affairs (QC/QA) Associate II What You'll Do as a (QC/QA)

Associate II:

ManufacturingBottling Quality Control (QC): Oversee production line clearances for both manufacturing and bottling operations. Ensure timely batch release, providing back-up support as needed. Review and approve document change requests. Maintain accuracy in part number assignment. Support the initiation, investigation, and resolution of complex deviations and CAPA reports. Design, support, and maintain the retention sample program, ensuring on-time finished product testing. Conduct label review and inspection to ensure compliance and accuracy. Support final product and raw material testing and release processes. Manage and monitor equipment calibration activities. Perform environmental monitoring, including monthly air, plate, and water sampling in manufacturing, bottling, and RO water systems. Quality Assurance (QA) /

Quality Affairs:

Manage product and customer complaints, including initiating and leading investigations through resolution. Maintain and administer the supplier qualification program. Support additional QA responsibilities as assigned.

What We're Looking For:

Applied Science or an Associate's degree in a comparable field 2 years of experience in a comparable field 2 years of cGMP experience MS Office Suite-intermediate skill level Must be able to walk, bend, stoop, and operate instrumentation requiring hand dexterity.

Preferred Qualifications:

3+ years of cGMP experience Bachelor's degree in a comparable field Experience with finished product testing and sampling Experience with 21 CFR Part 111 Dietary Supplements Technical writing experience (SOP, Regulatory submissions, technical reports)

Work EnvironmentSchedule:

Full-time, non-exempt position in a clean, regulated manufacturing environment and an office, with occasional short periods in a warehouse. Monday-Friday, 7:30 am-4:00 pm, with flexibility based on business needs.

Why You'll Love Working Here:

At Quicksilver Scientific, we're committed to supporting the health, well-being, and professional growth of our team. We offer a comprehensive benefits package that includes: Medical, Dental, and Vision Insurance Plans Health Savings Account (HSA)Flexible Spending Account (FSA) options Health Savings Account Match Company Paid Life, Short-TermLong-Term Disability Insurance 401(k) with up to 4% Company Match Four (4) weeks

Paid Time Off Gym Membership Reimbursement Compensation:

$30.00 to $33.00 per hour

About Quicksilver Scientific:

At Quicksilver Scientific, we believe in transforming health through science and innovation. Our mission is to help people live healthier, more vibrant lives with natural medicine that works. We are proud to foster a diverse, inclusive, and collaborative workplace. Ready to make an impact? Apply today and join a team where your expertise truly matters. Quicksilver Scientific is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.